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OncoMatch/Clinical Trials/NCT05284552

Tinzaparin And Biomarkers After Neoadjuvant Treatment of Ovarian Cancer

Is NCT05284552 recruiting? Yes, currently enrolling (Sep 2026). This Phase 2 trial studies Tinzaparin Injectable Solution for epithelial ovarian cancer.

Phase 2RecruitingUniversity Hospital, LinkoepingNCT05284552Data as of Sep 2026Location: Sweden

Treatment: Tinzaparin Injectable SolutionBackground: Previous findings have indicated antineoplastic properties of tinzaparin (Innohep®), a commonly used anti-coagulant. Earlier studies have mainly investigated the antineoplastic effects of tinzaparin in animal models and in human cell-lines. In this pilot study the aim is to examine the potential antitumoral effects of tinzaparin in vivo in women with epithelial ovarian cancer (EOC). Study objectives: Primary objective: The primary objective of the study is to evaluate the effects of tinzaparin on changes in levels of CA-125 in EOC patients who receive neoadjuvant chemotherapy (NACT). Secondary objectives: The secondary objective of the study is to explore the impact of tinzaparin on the dynamic of a spectrum of immunological and coagulation factors in EOC patients who receive NACT. Besides, the compliance of tinzaparin injections and adverse events caused by tinzaparin will be described.

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Extracted eligibility criteria

Treatments studied

Other

Tinzaparin Injectable Solution

Cancer type

Ovarian Cancer

Disease stage

Required: Stage FIGO III, FIGO IV (FIGO)

FIGO stage III-IV disease

Performance status

WHO 0–2

Demographics

Female only

Prior therapy

Cannot have received: warfarin

Concomitant treatment with heparins, low molecular weight heparins, warfarin or non-vitamin K antagonist oral anticoagulants

Lab requirements

Blood counts

Platelets <100 x10^9/L (analyzed no more than 14 days before start of treatment with investigational product)

Kidney function

E-GFR <30ml/min (analyzed no more than 14 days before start of treatment with investigational product)

E-GFR <30ml/min (analyzed no more than 14 days before start of treatment with investigational product); Platelets <100 x10^9/L (analyzed no more than 14 days before start of treatment with investigational product)

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT05284552 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior warfarin disqualifies patients from enrollment.

What disease stage is eligible?

Stage FIGO III or FIGO IV is required.

Is this trial open to male patients?

No. This trial enrolls female patients only.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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